S-3449 : Still Just a Bill


Registration of Certain Foreign Establishments Act

This bill expands statutory provisions that require foreign manufacturers of drugs or medical devices for the U.S. market to register with the Food and Drug Administration.

Specifically, if an establishment outside of the United States manufactures (or otherwise processes or prepares) a drug or medical device to be imported (or offered for import) into the United States, the establishment must comply with the registration requirements even if the drug or medical device in question undergoes further manufacturing at another non-U.S. establishment prior to importation into the United States.

Action Timeline

Action DateTypeTextSource
2022-01-10IntroReferralRead twice and referred to the Committee on Health, Education, Labor, and Pensions.Senate
2022-01-10IntroReferralIntroduced in SenateLibrary of Congress

Policy Area :

Health
Related Subjects
  • Administrative law and regulatory procedures
  • Drug safety, medical device, and laboratory regulation
  • Health technology, devices, supplies
  • Licensing and registrations
  • Manufacturing
Related Geographic Entities
Related Organizations
  • Department of Health and Human Services

Related Bills

See Related Bills